Resin batch
Material certification and batch identification.
Precision for
a healthier tomorrow.
Dedicated moulding capabilities, material experience and documented processes for medical and in-vitro diagnostics programmes.
Dedicated capabilityControlled processes.
Controlled processes.
Clear requirements.
The supplied profile describes 28 cleanroom moulding machines from 50T to 280T, with single-shot, insert, overmoulding and vertical moulding capabilities.
Explore inspection & validation ↗Application experienceComponents serving
Components serving
healthcare programmes.
The company profile identifies current and legacy programmes across these healthcare segments.
01
Endoscopy
02
Haemodialysis
03
Oxygen therapy
04
Airway management
05
Laboratory consumables
06
Life science
07
Ophthalmic
08
Urinary management
Medical polymer experienceMaterials are part
Materials are part
of the manufacturing conversation.
The profile lists experience with the following polymers. The exact grade, intended application and qualification requirements are reviewed for each programme.
PPPolypropylene
PCPolycarbonate
PVCIncluding DEHP-free PVC
LSRLiquid silicone rubber
TPE / TPUThermoplastic elastomers / polyurethane
PMMA / ABSAdditional polymer experience
LDPE / HDPEPolyethylene grades
K-Resin / TPS-SEBS / EVAAdditional materials listed in the profile
Material experience does not by itself establish suitability for a specific medical device or application.
Inside Nagoya
Materials in context.
Polymer and component imagery from the medical capability profile.
Medical polymers & component applications
Polymer materials and component applications.
Select a picture to explore it in more detail.
Traceability & change controlFollow the material.
Follow the material.
Control the change.
Production lot
Records linking material to the production lot.
Component identity
Laser Data Matrix Code marking where specified.
Change review
Documented review of material, process and supplier changes.
The marking format, record requirements and validation scope are agreed for each programme.
Programme introductionFrom development
From development
to a controlled production process.
New products and transfers follow a staged programme: scope review, DFM / DFA, tooling and first article, validation, then production handover.
Explore NPI & partner responsibilities ↗Planned expansion · Target Q2 2027
Additional ISO Class 8 assembly and cleanroom packaging capacity is described as a planned expansion. Existing production capability and the expansion programme are presented separately.
Additional ISO Class 8 assembly and cleanroom packaging capacity is described as a planned expansion. Existing production capability and the expansion programme are presented separately.
Your next manufacturing programme
Discuss your project ↗Let’s build what comes next.
Knowledge
Explore all guides ↗